Canonical Allele Identifier: CA971893099

Gene: FAH

Linked Data

• dbSNP Id: rs2041054257
• gnomAD v3: 15-80152502-GGGCTCGGGGA-G
• gnomAD v4: 15-80152502-GGGCTCGGGGA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.80152504_80152513del , CM000677.2:g.80152504_80152513del	GRCh38
NC_000015.9:g.80444846_80444855del , CM000677.1:g.80444846_80444855del	GRCh37
NC_000015.8:g.78231901_78231910del	NCBI36
NG_012833.1:g.4506_4515del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000558022.5:c.-71_-62del	ENSP00000453152.1:n.-71_-62del